Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.38 (A)
Location

Chromosome 9:78548557 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs61616381

HGVS name

9:g.78548557G>A

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant has 3989 sample genotypes and is mentioned in 2 citations.

Variant displays